Search Results - "Squire, J.A"
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First application of the Automated QUantitative Analysis (AQUA) technique to quantify PTEN protein expression in ovarian cancer: A correlative study of NCIC CTG OV.16
Published in Gynecologic oncology (01-03-2016)“…Abstract Background Platinum resistance is a dominant cause of poor outcomes in advanced ovarian cancer (OC). A mechanism of platinum resistance is the…”
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Genomic alterations detected by comparative genomic hybridization in ovarian endometriomas
Published in Brazilian journal of medical and biological research (01-08-2010)“…Endometriosis is a complex and multifactorial disease. Chromosomal imbalance screening in endometriotic tissue can be used to detect hot-spot regions in the…”
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High-resolution cDNA microarray CGH mapping of genomic imbalances in osteosarcoma using formalin-fixed paraffin-embedded tissue
Published in Cytogenetic and genome research (01-01-2004)“…Formalin-fixed paraffin embedded (FFPE) tumor tissue provides an opportunity to perform retrospective genomic studies of tumors in which chromosomal imbalances…”
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Cause and Consequences of Genetic and Epigenetic Alterations in Human Cancer
Published in Current genomics (01-09-2008)“…Both genetic and epigenetic changes contribute to development of human cancer. Oncogenomics has primarily focused on understanding the genetic basis of…”
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The Role of RUNX2 in Osteosarcoma Oncogenesis
Published in Sarcoma (2011)“…Osteosarcoma is an aggressive but ill-understood cancer of bone that predominantly affects adolescents. Its rarity and biological heterogeneity have limited…”
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Breast cancer 1 (BRCA1) protein expression as a prognostic marker in sporadic epithelial ovarian carcinoma: an NCIC CTG OV.16 correlative study
Published in Annals of oncology (01-11-2011)“…Breast cancer 1 (BRCA1) protein inactivation in sporadic ovarian carcinoma (OC) is common and low BRCA1 expression is linked with platinum sensitivity. The…”
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Genomic signatures of chromosomal instability and osteosarcoma progression detected by high resolution array CGH and interphase FISH
Published in Cytogenetic and genome research (01-01-2008)“…Osteosarcoma (OS) is characterized by an unstable karyotype which typically has a heterogeneous pattern of complex chromosomal abnormalities. High-resolution…”
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Topographical analysis of telomere length and correlation with genomic instability in whole mount prostatectomies
Published in The Prostate (15-05-2011)“…BACKGROUND Many critical events in prostatic carcinogenesis appear to relate to the emergence of genomic instability. Characteristic genomic abnormalities such…”
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Prostatic preneoplasia and beyond
Published in Biochimica et biophysica acta (01-04-2008)“…Prostate cancer is a heterogeneous neoplasm both with regard to its development, molecular abnormalities and clinical course. For example, in the United…”
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Correlating breakage-fusion-bridge events with the overall chromosomal instability and in vitro karyotype evolution in prostate cancer
Published in Cytogenetic and genome research (01-01-2007)“…Chromosomal instability (CIN) is thought to underlie the generation of chromosomal changes and genomic heterogeneity during prostatic tumorigenesis. The…”
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Integrated cytogenetic and high-resolution array CGH analysis of genomic alterations associated with MYCN amplification
Published in Cytogenetic and genome research (01-04-2011)“…Amplification of oncogenes and closely linked flanking genes is common in some types of cancer and can be associated with complex chromosome rearrangements…”
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Analysis of segmental duplications, mouse genome synteny and recurrent cancer-associated amplicons in human chromosome 6p21-p12
Published in Cytogenetic and genome research (01-06-2010)“…It has been proposed that regions of microhomology in the human genome could facilitate genomic rearrangements, copy number transitions, and rapid genomic…”
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The use of cytogenetics in understanding ovarian cancer
Published in Biomedicine & pharmacotherapy (2004)“…The future of cancer research is no longer limited to epidemiological data and clinical management, but rather encompasses a new dimension of understanding,…”
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Use of whole genome amplification and comparative genomic hybridisation to detect chromosomal copy number alterations in cell line material and tumour tissue
Published in Cytogenetic and genome research (2004)“…We have established that whole genome amplification (WGA), in conjunction with genomic DNA array comparative genomic hybridisation (gaCGH) allows for the…”
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Assignment of the human prostaglandin-endoperoxide synthase 2 (PTGS2) gene to 1q25 by fluorescence in situ hybridization
Published in Genomics (San Diego, Calif.) (01-10-1994)Get more information
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Mechanisms of loss of heterozygosity in retinoblastoma
Published in Cytogenetics and cell genetics (01-01-1992)“…Retinoblastoma (RB) tumors arise when both alleles of the RB1 gene are inactivated by two mutational events (M1 and M2). M1 can be an initial germline or…”
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Comparative genomic hybridization analysis of Y79 and FISH mapping indicate the amplified human mitochondrial ATP synthase alpha-subunit gene (ATP5A) maps to chromosome 18q12-->q21
Published in Cytogenetics and cell genetics (01-01-1997)“…The four mitochondrial ATP synthase alpha-subunit (ATP5A) genes map to chromosomes 2, 9, 16, and 18. In this study we have refined the localization of two of…”
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Chromosomal instability in osteosarcoma and its association with centrosome abnormalities
Published in Cancer genetics and cytogenetics (15-07-2003)“…The mechanism that generates the extreme aneuploidy that characterizes osteosarcoma (OS) is poorly understood. In this study, interphase fluorescence in situ…”
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